HS Awareness Support Group
Come join us at the Delta Hotels Toronto Airport & Conference Centre (International Room A) for our HS Awareness Support Group event! Connect with others who understand the challenges of living with HS. Share your experiences, learn coping strategies, and find support in a welcoming environment. Whether you're newly diagnosed or a long-time warrior, this group is here for you. Let's come together, share stories, uplift each other, and engage in self-care activities. Don't miss this opportunity to connect with your HS community, you are not alone. This event is sponsored by Novartis.
HS is a debilitating and painful chronic skin disease that currently does not have a cure. A formal diagnosis of this disease takes an average of 7years due to lack of knowledge and misdiagnosis which results in a high rate of depression and anxiety among the patients. Puberty is the onset of HS however recent research has indicated that HS is beginning to develop in children. 4% Canadians are affected by HS however, due to the lack the proper treatment in a timely manner one's quality of life is deeply affected.
Hidradenitis Suppurativa (HS) Awareness week this year is June 2-8th, 2024 where we spread awareness, educate, and come together with friends/family .
Hidradenitis and Me Support Group is a non-profit organization that provides a safe space for those who are living with Hidradenitis Suppurativa (HS). Our organization facilitates monthly support groups that focus on mental health and self-care with an objective to encourage others to live and enjoy life the best way they can, despite HS challenges.
